Regulation of cholesterol biosynthesis and lipid metabolism: A microRNA management perspective

被引:32
作者
Bhattarai, Asmita [1 ]
Likos, Eviania M. [1 ]
Weyman, Crystal M. [1 ]
Shukla, Girish C. [1 ]
机构
[1] Cleveland State Univ, Dept Biol Geo & EVS Sci, Ctr Gene Regulat, 2121 Euclid Ave, Cleveland, OH 44114 USA
关键词
Cholesterol biosynthesis; microRNA; Lipid metabolism; ELEMENT-BINDING PROTEIN; ACTIVATED RECEPTOR-GAMMA; LIVER-X-RECEPTOR; PRECURSOR PROTEIN; NUCLEAR RECEPTOR; IN-VIVO; ABCA1; EXPRESSION; GENE; LXR;
D O I
10.1016/j.steroids.2021.108878
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cellular disruption of lipid and cholesterol metabolism results in pathological processes linked to metabolic and cardiovascular diseases. Classically, at the transcription stages, the Cholesterol levels are controlled by two cellular pathways. First, the SREBP transcription factor family controls Cholesterol biosynthesis via transcriptional regulation of critical rate-limiting cholesterogenic and lipogenic proteins. Secondly, The LXR/RXR transcription factor family controls cholesterol shuttling via transcriptional regulation of cholesterol transport proteins. In addition, the posttranscriptional control of gene expression of various enzymes and proteins of cholesterol biosynthesis pathways is mediated by small non-coding microRNAs. Regulatory noncoding miRNAs are critical regulators of biological processes, including developmental and metabolic functions. miRNAs function to fine-tune lipid and cholesterol metabolism pathways by controlling the mRNA levels and translation of critical molecules in each pathway. This review discusses the regulatory roles of miRNAs in cholesterol and lipid metabolism via direct and indirect effects on their target genes, including SREBP, LXR, HDL, LDL, and ABCA transporters. We also discuss the therapeutic implications of miRNA functions and their purported role in the potentiation of small molecule therapies.
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页数:10
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